Trabajos Science en NY

Job DescriptionCompany Description The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you’re looking for a rewarding career, apply with us today! Job Description Eurofins PSS is seeking a Lead Analytical Chemist to oversee and support laboratory operations in a GMP-regulated pharmaceutical environment. This role combines hands-on analytical testing with team leadership responsibilities, ensuring high-quality data generation, compliance, and operational efficiency. You’ll lead a team performing routine and technical testing, support process science and technical transfers, and ensure all lab activities meet regulatory and quality standards. Key Responsibilities Laboratory Responsibilities • Perform and support analytical testing of pharmaceutical products, including UV-Vis/Solo-VPE, pH, density, and osmolality., • Assist with technical transfer testing for development teams., • Conduct real-time checks and verifications of lab tasks., • Coordinate routine equipment maintenance, cleaning, and calibration., • Use electronic systems to document sample handling, procedures, and data., • Ensure documentation complies with GDP and ALCOA+ principles., • Review test results and logbooks for accuracy and compliance., • Maintain clean, organized, and properly labeled lab spaces., • Interact professionally with internal teams and external customers., • Manage daily workload and scheduling for the lab team., • Conduct 1:1 meetings and lead team huddles., • Monitor and report productivity and quality metrics., • Perform safety walkthroughs and compliance checks., • Participate in hiring, onboarding, and training of new team members., • Deliver training to new hires and existing staff., • Support weekend and overtime scheduling as needed.Qualifications, • Bachelor’s degree in Life Sciences or a related field., • At least 2 years of leadership experience in a laboratory setting., • Hands-on experience with analytical methods such as UV-Vis/Solo-VPE, pH, density, and osmolality., • Strong understanding of cGMP and laboratory compliance standards., • Excellent communication, organizational, and documentation skills., • Ability to work independently and collaboratively in a fast-paced environment., • Physically able to lift 25+ lbs, stand for extended periods, and perform routine lab tasks., • Authorized to work in the U.S. without restriction or sponsorship. Additional Information What to Expect in the Hiring Process: • 10-15 Minute Phone Interview with Region Recruiter, • 45-60 Minute Virtual Interview with Manager and/or Group Leader, • Excellent full-time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our clients’ quality systems and equipment. To learn more about Eurofins Lancaster Laboratories, please explore our website . Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing If you’re looking for a rewarding career, apply with us today! Job Description Eurofins PSS is seeking an Analytical Chemist – Mass Spectrometry Specialist to support extractables and leachables (E&L) testing for pharmaceutical manufacturing. This role involves hands-on work with GC-MS, LC-MS, and/or ICP-MS in a GMP-regulated lab, supporting both clinical and commercial testing. You’ll be responsible for generating and interpreting complex data, troubleshooting instrumentation, and ensuring compliance with all regulatory and quality standards. Key Responsibilities • Perform E&L testing using GC-MS, LC-MS, and/or ICP-MS., • Follow all relevant protocols, SOPs, and cGxP guidelines., • Analyze and interpret complex data; compile results into technical summary documents., • Review test results for accuracy and compliance; report any anomalies., • Calibrate and verify instruments before use., • Troubleshoot instrumentation and lab techniques as needed., • Support method validation and continuous improvement efforts., • Maintain lab supplies, safety standards, and documentation., • Participate in training activities as both a trainee and a trainer., • Interact professionally with vendors and cross-functional teams.Qualifications, • Bachelor’s degree in Chemistry or a related scientific field with 2+ years of industry experience, or a Master’s degree with any industry experience., • Hands-on experience with GC-MS, LC-MS, and/or ICP-MS., • Experience working in a GMP-regulated laboratory., • Strong skills in data analysis, documentation, and technical writing., • Familiarity with electronic laboratory information management systems (LIMS)., • Excellent attention to detail, communication skills, and ability to work independently or in a team., • Must be authorized to work in the U.S. without restriction or sponsorship. Additional Information What to Expect in the Hiring Process: • 10-15 Minute Phone Interview with Region Recruiter The position is full-time, first shift, Monday-Friday from 8am-4:30pm. Candidates must be flexible to adapt to schedule changes requiring shift changes and/or weekend work, and overtime may be required as needed. Candidates living within a commutable distance of Rensselaer, New York, are encouraged to apply. Excellent full-time benefits include: • comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holiday, • Yearly goal-based bonus & eligibility for merit-based increases We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment. To learn more about Eurofins Lancaster Laboratories, please explore our website . Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description We are seeking an experienced Paint Chemist in Yonkers, NY! This is a temp to perm role offers $33.65/hour (~$70K annually) plus a $5,000 sign-on bonus. The ideal candidate has expertise in polymers, coatings, inks, or paint formulations and will lead product development and testing. Apply today to join a growing team with excellent career opportunities! About the Opportunity We are a staffing agency seeking an experienced Paint Chemist to join a fast-paced and innovative manufacturing team in Yonkers, NY. The ideal candidate will bring hands-on expertise in polymers, coatings, inks, and paint formulations to support product development, testing, and improvement of high-performance coatings. This is a direct-hire opportunity with competitive pay and a $5,000 sign-on bonus. Key Responsibilities * Develop, test, and optimize paint, coatings, and polymer formulations. * Conduct laboratory analysis on raw materials and finished products. * Ensure compliance with industry standards and regulatory guidelines. * Collaborate with production teams to scale lab formulations to manufacturing. * Troubleshoot performance issues and recommend technical solutions. * Maintain accurate records of experiments, formulations, and results. Qualifications * Minimum 3–5 years of experience in paint, coatings, polymers, or ink formulation. * Strong knowledge of raw materials, additives, and application techniques. * Ability to operate and interpret results from lab testing equipment. * Excellent problem-solving, communication, and organizational skills. * Bachelor’s degree in Chemistry, Polymer Science, Materials Science, or related field (advanced degree preferred). Compensation & Benefits * Pay: $33.65/hour (~$70,000 annually). * $5,000 Sign-On Bonus. * Full-time, direct-hire role with growth opportunities. Why Work With Us As a staffing agency, we connect top talent with outstanding employers. We advocate for our candidates and ensure they’re placed in roles that align with their skills, experience, and career goals. When you work with us, you gain access to exclusive opportunities, personalized recruiter support, and direct connections to companies looking for your expertise. How to Apply Interested candidates should submit their resume through ZipRecruiter for immediate consideration. A recruiter will contact qualified applicants directly with next steps. Equal Employment Opportunity We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, veteran status, gender identity, sexual orientation, or any other characteristic protected by law.

Job Description Job Summary The Chemist II, under minimal supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability and finished products, and testing to support process validation. Has demonstrated competence in conducting all types of physical and chemical analyses (including complex analyses) using all equipment. Detects, conducts, and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. Participates in troubleshooting analyses and instrumentation. Trains less senior staff. Analysis & Testing • Conducts laboratory analyses according to approved test methods: finished product testing, stability testing, raw material testing, cleaning verification testing and manufacturing in-process testing. Typical activities may include buffer/solution preparation, standard preparation and operating analytical instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc., • Uses laboratory software for analyses, • Reviews and approves laboratory test data and documentation for completeness and compliance, • Is alert to and detects abnormalities during performances of tests and reviews. Elevates abnormalities to Supervisor, • Provides general laboratory support such as routine instrument cleaning/preventative maintenance/calibration, sample receiving, chemical inventory, document filing and housekeeping, • Cleans lab working surfaces and dispose of any excess chemicals, solutions, solvents, etc. in the special waste containers for each class of waste chemicals, • Detects, conducts and reports on OOS/OOT/NOE and other investigations, • Elevates questionable sample results, OOS, and aberrant results immediately to Supervisor and recommends a course of action, • Maintains assigned training records current and in-compliance, • Performs assigned work in a timely and safe manner conforming to regulatory, company and compendiaI requirements within pharmaceutical manufacturing setting, • Document accurately data generated in notebooks/worksheets/LIMS in compliance with SOPs, • Follows EH&S procedures to ensure a safe work environment Education & Experience Minimal acceptable level of education, work experience and certifications required for the job • Bachelor of Science Degree in chemistry, chemical engineering or related field with 4+ years’ relevant analytical laboratory experience OR Proficiency in a body of information required for the job e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc. • Has strong knowledge of laboratory software and has expanded knowledge of chromatographic software (e.g. Waters Empower, Agilent ChemStation and Sotax WinSotax), using custom fields, custom calculations and custom reports, • Full proficiency with various laboratory techniques/instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc., • Thorough knowledge of applicable safety and standards guidelines, such as SOP, cGMP, GLP, DEA regulations and/or MSDS, • Has demonstrated competence in conducting chemical analyses, • Strong knowledge of wet chemistry techniques & Abilities Often referred to as “competencies”, leadership attributes, skills, abilities or behaviors that may be enterprise, functional or job specific e.g. coaching, negotiation, calibration, technical writing etc. • Ability to critically review and analyze data, interpret information, and draw conclusions from relevant or missing information, reporting to management, • Ability to display and analyze data in a logical manner, • Ability to critically review, analyze data, interpret information, and draw conclusions from relevant or missing information, • Ability to display and analyze data in a logical manner, • Strong verbal and written communication skills as well as good computer skills, • Strong attention to details and accurate record keeping, • Establish and maintain cooperative working relationships with others, • Solid organizational skills, • Ability to coach less senior staff and develop laboratory skills and ability Physical & mental requirements e.g., lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc. • Extended periods of sitting, standing, walking, reaching, climbing/balancing, kneeling/crouching/crawling, looking at monitor for extended periods, moderate noise levels and potential business travel. Work is in an FDA and DEA-regulated pharma lab environment with risk of exposure to various chemicals, • Must occasionally lift and/or move up to 15-25 lbs., • Ability to wear personal protective equipment, including respirators, gloves, etc., • Specific visions abilities are required by this job include close vision and color vision, • Ability to occasionally tolerate significant differences in temperature and/or humidity for short periods

Job Title: Analytical Chemist Department: Quality Control Location: Queensbury, NY Reports To: Quality Control Supervisor FLSA Status: Salaried Date Prepared: May 2025 POSITION SUMMARY The Chemist will play a critical role in product release testing and will participate in QC/ R&D activities related to product development. The incumbent must demonstrate a high level of involvement in continuous improvement activities to ensure the highest standards are maintained. The Chemist must possess the ability to solve practical problems and deal with a variety of situations in a fast-paced environment. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. • Assist with the end-to-end process of batch release testing which includes but not limited to preparation of drug solution, sample collection, data review/ analysis, and other., • Proactively take measures to ensure that all equipment is current with calibration and PM services, where applicable., • Comply with GDPs for maintenance of data and records. Maintain knowledge of organizational SOPs and apply where needed., • Participate in developing and validating QC test methods while complying with Quality Management Systems (QMS), in accordance with ISO standards and regulatory requirements., • Responsible for R&D activities including writing/ executing protocols, preparing standards/ reagents/ solutions, analysis of samples using LC-MS on a routine basis., • Responsible for maintaining the LC-MS instrument per set requirements., • Assist with effective planning and organizing of R&D lab activities to meet set project deliverables. Collaborate with peers/ external teams to organize and conduct research., • Comprehend, and effectively communicate technical data across cross-functional teams. SUPERVISORY RESPONSIBILITIES None. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE · A minimum of bachelor’s degree in chemistry or life sciences is required. · Knowledge and experience working in Quality Control is required. · Must be instrumental with UPLC-MS/MS with an experience in MassLynx application software and method development techniques. A minimum of 2 years’ experience is required. · Ability to effectively identify/ trouble shoot instrument related technical problems, as needed. · Ability to read, understand, and conduct USP/NF raw materials official monograph testing is required. · Ability to read and understand peer reviewed journals/ research articles. · Must possess strong analytical problem solving and process skills, and be computer proficient in EXCEL, Word, etc. · Must be willing to learn any new application as needed. · Must be team oriented, with the ability to work well with diverse cross-functional teams. · Must possess strong verbal and written communication skills. · Must possess ability to apply common sense understanding to carry out instructions in written, oral, or schematic form. LANGUAGE SKILLS Ability to read and interpret documents such as technical journals, safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively with employees and outside organizations. MATHEMATICAL SKILLS Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and create and/or interpret spreadsheets and graphs. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit. The employee is frequently required to use hands to finger, handle, or feel and reach with hands and arms; and is subject to repetitive motions of the wrists, hands, and/or fingers. The employee must occasionally lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception, and ability to adjust focus. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts, heat, airborne particles, moderate noise and outside weather conditions.

Chemist Location: New York City; Clark, NJ; Tampa, FL Employment Type: Contract Department: Reporting To: Program Manager About Cogent Infotech At Cogent Infotech, we believe in creating opportunities that empower individuals and transform organizations.

Qualification Requirements A baccalaureate degree from an accredited college, including or supplemented by 16 semester credits in chemistry and 8 semester credits in any one or a combination of the following areas: chemistry, pharmacology, toxicology, environmental science, forensic science, or othe

Qualification Requirements A baccalaureate degree from an accredited college, including or supplemented by 16 semester credits in chemistry and 8 semester credits in any one or a combination of the following areas: chemistry, pharmacology, toxicology, environmental science, forensic science, or othe

The candidate will work within a team of synthetic chemists and be expected to lead their program throughout the internship. The candidate must be actively enrolled in an undergraduate or graduate program at the time of application and for at least one semester following the conclusion of the intern

Qualification Requirements A baccalaureate degree from an accredited college, including or supplemented by 16 semester credits in chemistry and 8 semester credits in any one or a combination of the following areas: chemistry, pharmacology, toxicology, environmental science, forensic science, or othe

A major client of ours has a need for a QC Chemist for their Hauppauge, NY location.

The job of the "Chemist" is simple described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The general duties and responsibilities of the "Chemist" include but are not limited to the following:.

Functional knowledge of laboratory equipment and techniques. Work is performed in a laboratory setting with routine exposure to hazardous materials.